<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Liu J</submitter><funding>National High Level Hospital Clinical Research Funding</funding><funding>Beijing Municipal Science &amp; Technology Commission</funding><funding>CAMS Innovation Fund for Medical Sciences</funding><funding>National Natural Science Foundation of China</funding><funding>National Key Research and Development Program of China</funding><funding>Beijing Natural Science Foundation</funding><pagination>519-531</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10270746</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(6)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Glucokinase maturity-onset diabetes of the young (GCK-MODY) is difficult to distinguish from other diabetic forms. This article aims to characterize the differences in results from routine examinations between GCK-MODY and hepatocyte nuclear factor 1-α (HNF1A)-MODY or type 2 diabetes (T2D) patients in different periods of diabetes.&lt;h4>Methods&lt;/h4>Ovid Medline, Embase, and the Cochrane Library were searched up until October 9, 2022 for articles containing baseline characteristics of GCK-MODY, HNF1A-MOFY, and T2D, excluding pregnant women. The pooled standardized mean differences were derived using a random-effects model.&lt;h4>Results&lt;/h4>Compared to HNF1A-MODY, GCK-MODY patients had lower indicators of glucose metabolism. Total triglycerides (TG) (-0.93 [-1.66, -0.21] mmol/</pubmed_abstract><journal>Journal of diabetes</journal><pubmed_title>Insights from basic adjunctive examinations of GCK-MODY, HNF1A-MODY, and type 2 diabetes: A systemic review and meta-analysis.</pubmed_title><pmcid>PMC10270746</pmcid><funding_grant_id>2018YFC2001100</funding_grant_id><funding_grant_id>2022-PUMCH-B-121</funding_grant_id><funding_grant_id>82170854</funding_grant_id><funding_grant_id>CIFMS2017-I2M-1-008</funding_grant_id><funding_grant_id>7202163</funding_grant_id><funding_grant_id>81570715</funding_grant_id><funding_grant_id>CIFMS2021-1-I2M-002</funding_grant_id><funding_grant_id>81170736</funding_grant_id><funding_grant_id>Z201100005520011</funding_grant_id><funding_grant_id>2022-PUMCH-C-019</funding_grant_id><funding_grant_id>81870545</funding_grant_id><funding_grant_id>81870579</funding_grant_id><pubmed_authors>Liu J</pubmed_authors><pubmed_authors>Yu M</pubmed_authors><pubmed_authors>Xiao X</pubmed_authors><pubmed_authors>Zhang Q</pubmed_authors></additional><is_claimable>false</is_claimable><name>Insights from basic adjunctive examinations of GCK-MODY, HNF1A-MODY, and type 2 diabetes: A systemic review and meta-analysis.</name><description>&lt;h4>Background&lt;/h4>Glucokinase maturity-onset diabetes of the young (GCK-MODY) is difficult to distinguish from other diabetic forms. This article aims to characterize the differences in results from routine examinations between GCK-MODY and hepatocyte nuclear factor 1-α (HNF1A)-MODY or type 2 diabetes (T2D) patients in different periods of diabetes.&lt;h4>Methods&lt;/h4>Ovid Medline, Embase, and the Cochrane Library were searched up until October 9, 2022 for articles containing baseline characteristics of GCK-MODY, HNF1A-MOFY, and T2D, excluding pregnant women. The pooled standardized mean differences were derived using a random-effects model.&lt;h4>Results&lt;/h4>Compared to HNF1A-MODY, GCK-MODY patients had lower indicators of glucose metabolism. Total triglycerides (TG) (-0.93 [-1.66, -0.21] mmol/</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jun</publication><modification>2025-04-22T18:52:44.384Z</modification><creation>2025-04-06T02:33:59.539Z</creation></dates><accession>S-EPMC10270746</accession><cross_references><pubmed>37226652</pubmed><doi>10.1111/1753-0407.13390</doi></cross_references></HashMap>